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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 964968생성일: 2026년 10월 25일

Triphenylphosphine → methyl (RS)-3-(1-cyclopropyl-prop-2-ynyloxy)-4,5-dimethoxy-benzoate

https://huagongshe.com/reaction/964968

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물1-Cyclopropylprop-2-yn-1-olHCID 343119—
반응물Methyl 3-hydroxy-4,5-dimethoxybenzoateHCID 2733956—
용매TolueneHCID 1140—
생성물methyl (RS)-3-(1-cyclopropyl-prop-2-ynyloxy)-4,5-dimethoxy-benzoateHCID 54377500—

반응 조건

온도5 °C

반응 단계

63.6 g of methyl 3,4-dimethoxy-5-hydroxy-benzoate [E. Spath and H. Roder, Monatsh. fur Chemie, 43, 93 (1923)], 38.5 g of (RS)-1-cyclopropyl-prop-2-yn-1-ol and 118 g of triphenylphosphine were dissolved in 600 ml of toluene under argon and cooled to 5° C. A solution of 70 ml of diethyl azodicarboxylate in 150 ml of toluene was slowly added dropwise thereto at 5° C. over 90 min. The mixture was stirred at 5° C. for a further 1 hr. and at 20° C. for 3 hrs. Then, 300 ml of toluene were distilled off on a rotary evaporator and the suspension obtained was stirred in an ice bath for 30 min. The separated triphenylphosphine oxide was filtered off and the filtrate was evaporated. The resulting oil was chromatographed on silica gel with hexane/ethyl acetate 4:1, then 3:1. Crystallization was effected from diethyl ether and hexane. There was obtained methyl (RS)-3-(1-cyclopropyl-prop-2-ynyloxy)-4,5-dimethoxy-benzoate as white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05773446
출처 데이터셋uspto-grants-1998_06
ORD IDord-26a6e4fe57844be886e38b37d5444c66
출처 메모uspto-grants-1998_06